DMSO and iodine mediated reaction of 4-hydroxycoumarins and aldehydes/aryl methyl ketones: synthesis of furo[3,2-c]coumarins
作者:Sinki Kolita、Pallabi Borah、P. Seetham Naidu、Pulak J. Bhuyan
DOI:10.1016/j.tet.2015.12.016
日期:2016.1
and efficient method for the synthesis of highly functionalized furo[3,2-c]coumarins was developed. The reaction occurred via initial formation of biscoumarins from the reaction of 4-hydroxycoumarins and aldehydes/aryl methyl ketones in the presence of molecular iodine in DMSO followed by lactone ring opening, cyclization and oxidative aromatization process. The reaction conditions were moderate, work-up
开发了一种简单高效的合成高度官能化的呋喃[3,2- c ]香豆素的方法。该反应是在DMSO中存在分子碘的情况下,由4-羟基香豆素与醛/芳基甲基酮的反应最初生成双香豆素而发生的,然后是内酯开环,环化和氧化芳构化过程。反应条件温和,后处理步骤简单,并且以高收率获得产物。
Synthesis of furo[3,2-<i>c</i>]coumarin from the reaction of 3-halochromone and 2-aminochromone; 2-aminochromone as a masked 4-hydroxycoumarin
Synthesis of 2-(2-hydroxybenzoyl)-4H-furo[3,2-c]chromen-4-one has been accomplished by the reaction of 3-halochromone with 2-aminochromone. In this reaction, 2-aminochromone acts as a masked 4-hydroxycoumarin.